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UK approves Pfizer and BioNTech’s COVID-19 vaccine for emergency use
High-Throughput a1-Acid Glycoprotein Binding Assay
AI Innovation Lab, BioNTech and InstaDeep, London and Mainz
FDA approves Roche’s Xofluza for Influenza post-exposure prophylaxis
Mouse Specific CD19 Antibody

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FDA approves Roche’s Venclexta combos for acute myeloid leukaemia

October 22, 2020October 24, 2020 Pharmaceutical Industry Editor

Roche revealed on Monday that Venclexta ® (venetoclax) in conjunction with azacitidine or decitabine or low-dose cytarabine (LDAC) has been

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UK approves Pfizer and BioNTech’s COVID-19 vaccine for emergency use

December 2, 2020December 3, 2020 Pharmaceutical Industry Editor

The UK has become the first western country to approve Pfizer and BioNTech’s COVID-19 vaccine for emergency use. The United

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The 20 min high-throughput assay estimates the binding of drugs to a1-acid glycoprotein (AGP) and is essential for predicting plasma

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